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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 584 European ancestry cases, 6,040 European ancestry controls.
The effect
Each copy of the G allele carried 2.98 times the odds of Non-alcoholic chronic pancreatitis (95% confidence interval 2.10873513370054-4.21788937849748); p = 6 × 10−10.
How common The G allele had a frequency of about 3% in the people studied.
Where it sits Chromosome 5, band 5q32 — in an intron of JAKMIP2-AS1.
What each result means
A/ANo copy of the version the research linked to Non-alcoholic chronic pancreatitis. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Non-alcoholic chronic pancreatitis. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Non-alcoholic chronic pancreatitis. That is the strongest link of the three results. A link in a study is not a diagnosis.
Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2022 · PMID 35331647
Questions about rs146303903
What is rs146303903?
rs146303903 is a single position in the genome, in or near the JAKMIP2-AS1 gene. Published research associates it with non-alcoholic chronic pancreatitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs146303903 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs146303903 come from?
GWAS Catalog, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2022, PMID:35331647. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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